The DOI matches its Crossref record; 119 of the 119 references it cites were found in a registry or an index.
The Emerging Science of Interoception: Sensing, Integrating, Interpreting, and Regulating Signals within the Self
Open accessAbstract
Interoception refers to the representation of the internal states of an organism, and includes the processes by which it senses, interprets, integrates, and regulates signals from within itself. This review presents a unified research framework and attempts to offer definitions for key terms to describe the processes involved in interoception. We elaborate on these definitions through illustrative research findings, and provide brief overviews of central aspects of interoception, including the anatomy and function of neural and non-neural pathways, diseases and disorders, manipulations and interventions, and predictive modeling. We conclude with discussions about major research gaps and challenges.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“From a PNE perspective, interoceptive skills-building helps the person notice relationships between inputs (physiology, and BPS factors that influence threat or safety), and the output/experience of pain.58,59”
From Remotely Delivered Psychologically Informed Mindful Movement Physical Therapy for Pain Care: A Framework for Operationalization (2023) · cites this paper as [58]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“These insights empower the person to recognize their own unique triggers with less judgement, to build trust in themselves, and to find ways to change the relationships and reactions to these bodily activations.”
From Remotely Delivered Psychologically Informed Mindful Movement Physical Therapy for Pain Care: A Framework for Operationalization (2023) · cites this paper as [58]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The interoceptive sensation is mediated by two primary ascending neural pathways: the spinal nerve pathway and the vagal nerve pathway [55].”
From The Insular Cortex: An Interface Between Sensation, Emotion and Cognition (2024) · cites this paper as [55]
In the citing paper
“Interoception impairment (i.e., difficulties in the sensing, perceiving, and anticipating of signals arising from within the body) is a core feature that can occur in multiple clinical conditions.1, 2, 3”
From Altered spatiotemporal brain dynamics of interoception in behavioural-variant frontotemporal dementia (2025) · cites this paper as [2]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657
How do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006
Neural systems supporting interoceptive awareness
Critchley, H. D., Wiens, S., Rotshtein, P., Öhman, A., & Dolan, R. J. (2004) · Nature Neuroscience · doi:10.1038/nn1176 · Cited by 3,406
Interoception and Mental Health: A Roadmap.
Khalsa, S. S., Adolphs, R., Cameron, O. G., Critchley, H. D., Davenport, P. W., Feinstein, J. S., Feusner, J. D., Garfinkel, S. N., Lane, R. D., Mehling, W. E., et al. (2018) · Biological psychiatry. Cognitive neuroscience and neuroimaging · doi:10.1016/j.bpsc.2017.12.004 · Cited by 1,453
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Kurth, F., Zilles, K., Fox, P. T., Laird, A. R., & Eickhoff, S. B. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0255-z · Cited by 1,293
Structure and Function of the Human Insula
Uddin, L. Q., Nomi, J. S., Hébert-Seropian, B., Ghaziri, J., & Boucher, O. (2017) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000377 · Cited by 1,262
Visceral influences on brain and behavior
Critchley, H. D., & Harrison, N. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.008 · Cited by 1,177
Insula of the old world monkey. III: Efferent cortical output and comments on function
Mesulam, M. ‐., & Mufson, E. J. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902120104 · Cited by 1,013
Piezo2 is the major transducer of mechanical forces for touch sensation in mice
Ranade, S. S., Woo, S., Dubin, A. E., Moshourab, R. A., Wetzel, C., Petrus, M. J., Mathur, J., Bégay, V., Coste, B., Mainquist, J. K., et al. (2014) · Nature · doi:10.1038/nature13980 · Cited by 953
An Interoceptive Predictive Coding Model of Conscious Presence
Seth, A. K., Suzuki, K., & Critchley, H. D. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00395 · Cited by 950
A gut-brain neural circuit for nutrient sensory transduction
Kaelberer, M. M., Buchanan, K. L., Klein, M. E., Barth, B. B., Montoya, M. M., Shen, X., & Bohórquez, D. V. (2018) · Science · doi:10.1126/science.aat5236 · Cited by 932
Ehde, D. M., Dillworth, T. M., & Turner, J. A. (2014) · American Psychologist · doi:10.1037/a0035747 · Cited by 879
Gogolla, N. (2017) · Current Biology · doi:10.1016/j.cub.2017.05.010 · Cited by 851
The central autonomic nervous system: conscious visceral perception and autonomic pattern generation
Saper, C. B. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.032502.111311 · Cited by 837
A Neural Circuit for Gut-Induced Reward
Han, W., Téllez, L. A., Perkins, M. H., Pérez-Martínez, I. O., Qu, T., Ferreira, J. G. P., Ferreira, T. L., Quinn, D., Liu, Z.-W., Gao, X., et al. (2018) · Cell · doi:10.1016/j.cell.2018.08.049 · Cited by 772
Anterior insular cortex and emotional awareness
Gu, X., Hof, P. R., Friston, K. J., & Fan, J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23368 · Cited by 712
Evidence for a viscerotopic sensory representation in the cortex and thalamus in the rat
Cechetto, D. F., & Saper, C. B. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620104 · Cited by 703
Mesulam, M. M., & Mufson, E. J. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902120102 · Cited by 660
Sensory neurons that detect stretch and nutrients in the digestive system
Williams, E. K., Chang, R. B., Strochlic, D. E., Umans, B. D., Lowell, B. B., & Liberles, S. D. (2016) · Cell · doi:10.1016/j.cell.2016.05.011 · Cited by 645
The neurocircuitry of impaired insight in drug addiction
Goldstein, R. Z., Craig, A. D. (., Bechara, A., Garavan, H., Childress, A. R., Paulus, M. P., & Volkow, N. D. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.06.004 · Cited by 641
Evidence for a large-scale brain system supporting allostasis and interoception in humans
Kleckner, I. R., Zhang, J., Touroutoglou, A., Chanes, L., Xia, C., Simmons, W. K., Quigley, K. S., Dickerson, B. C., & Feldman Barrett, L. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0069 · Cited by 641
Chapter 4 Affect as a Psychological Primitive
Barrett, L. F., & Bliss‐Moreau, E. (2009) · Advances in Experimental Social Psychology · doi:10.1016/s0065-2601(08)00404-8 · Cited by 621
THE INSULA: FURTHER OBSERVATIONS ON ITS FUNCTION
PENFIELD, W., & FAULK, M. E. (1955) · Brain · doi:10.1093/brain/78.4.445 · Cited by 606
Insula of the old world monkey. II: Afferent cortical input and comments on the claustrum
Mufson, E. J., & Mesulam, M. ‐. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902120103 · Cited by 559
Interoception: The Inside Story—A Model for Psychosomatic Processes
Cameron, O. G. (2001) · Psychosomatic Medicine · doi:10.1097/00006842-200109000-00001 · Cited by 535
Discrepancies between dimensions of interoception in autism: implications for emotion and anxiety
Garfinkel, S. N., Tiley, C., O'Keeffe, S., Harrison, N. A., Seth, A. K., & Critchley, H. D. (2016) · Biological Psychology · doi:10.1016/j.biopsycho.2015.12.003 · Cited by 512
Tuthill, J. C., & Azim, E. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.064 · Cited by 480
The Role of PIEZO2 in Human Mechanosensation
Chesler, A. T., Szczot, M., Bharucha-Goebel, D., Čeko, M., Donkervoort, S., Laubacher, C., Hayes, L. H., Alter, K., Zampieri, C., Stanley, C., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1602812 · Cited by 462
An Atlas of Vagal Sensory Neurons and Their Molecular Specialization
Kupari, J., Häring, M., Agirre, E., Castelo‐Branco, G., & Ernfors, P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.096 · Cited by 444
Avery, J. A., Drevets, W. C., Moseman, S. E., Bodurka, J., Barcalow, J. C., & Simmons, W. K. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.11.027 · Cited by 442
Vagal Sensory Neuron Subtypes that Differentially Control Breathing
Chang, R. B., Strochlic, D. E., Williams, E. K., Umans, B. D., & Liberles, S. D. (2015) · Cell · doi:10.1016/j.cell.2015.03.022 · Cited by 441
The anterior insula in autism: Under-connected and under-examined
Uddin, L. Q., & Menon, V. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.06.002 · Cited by 432
Neural circuits of interoception
Berntson, G. G., & Khalsa, S. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.011 · Cited by 419
Visceral Signals Shape Brain Dynamics and Cognition
Azzalini, D., Rebollo, I., & Tallon-Baudry, C. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.03.007 · Cited by 409
The Spinothalamic System Targets Motor and Sensory Areas in the Cerebral Cortex of Monkeys
Dum, R. P., Levinthal, D. J., & Strick, P. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3398-09.2009 · Cited by 408
The pathways of interoceptive awareness
Khalsa, S. S., Rudrauf, D., Feinstein, J. S., & Tranel, D. (2009) · Nature Neuroscience · doi:10.1038/nn.2411 · Cited by 387
A convergent functional architecture of the insula emerges across imaging modalities
Kelly, C., Toro, R., Di Martino, A., Cox, C. L., Bellec, P., Castellanos, F. X., & Milham, M. P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.021 · Cited by 374
Evolving pathophysiologic models of functional gastrointestinal disorders
Mayer, E. A., & Collins, S. M. (2002) · Gastroenterology · doi:10.1053/gast.2002.33584 · Cited by 329
Rinaman, L. (2010) · Brain Research · doi:10.1016/j.brainres.2010.03.059 · Cited by 311
Towards a psychophysics of interoceptive processes: the measurement of heartbeat detection
Brener, J., & Ring, C. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0015 · Cited by 307
Aversive state processing in the posterior insular cortex
Gehrlach, D. A., Dolensek, N., Klein, A. S., Roy Chowdhury, R., Matthys, A., Junghänel, M., Gaitanos, T. N., Podgornik, A., Black, T. D., Reddy Vaka, N., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0469-1 · Cited by 303
Harshaw, C. (2015) · Psychological Bulletin · doi:10.1037/a0038101 · Cited by 302
Threat and the body: how the heart supports fear processing
Garfinkel, S. N., & Critchley, H. D. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.005 · Cited by 298
Kanoski, S. E., & Grill, H. J. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.09.011 · Cited by 294
Functions of interoception: From energy regulation to experience of the self
Quigley, K. S., Kanoski, S., Grill, W. M., Barrett, L. F., & Tsakiris, M. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.008 · Cited by 286
Mufson, E. J., & Mesulam, M. M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902270112 · Cited by 275
Differentiating attention styles and regulatory aspects of self-reported interoceptive sensibility
Mehling, W. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0013 · Cited by 261
A role of insular cortex in cardiovascular function
Ruggiero, D. A., Mraovitch, S., Granata, A. R. M., Anwar, M., & Reis, D. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902570206 · Cited by 260
Diseases, Disorders, and Comorbidities of Interoception
Bonaz, B., Lane, R. D., Oshinsky, M. L., Kenny, P. J., Sinha, R., Mayer, E. A., & Critchley, H. D. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.009 · Cited by 260
Interventions and Manipulations of Interoception
Weng, H. Y., Feldman, J. L., Leggio, L., Napadow, V., Park, J., & Price, C. J. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.010 · Cited by 250
The Organization of the Primate Insular Cortex
Evrard, H. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00043 · Cited by 242
Computational Models of Interoception and Body Regulation
Petzschner, F. H., Garfinkel, S. N., Paulus, M. P., Koch, C., & Khalsa, S. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.012 · Cited by 227
Gut vagal sensory signaling regulates hippocampus function through multi-order pathways
Suarez, A. N., Hsu, T. M., Liu, C. M., Noble, E. E., Cortella, A. M., Nakamoto, E. M., Hahn, J. D., de Lartigue, G., & Kanoski, S. E. (2018) · Nature Communications · doi:10.1038/s41467-018-04639-1 · Cited by 212
Interoceptive awareness declines with age
Khalsa, S. S., Rudrauf, D., & Tranel, D. (2009) · Psychophysiology · doi:10.1111/j.1469-8986.2009.00859.x · Cited by 211
Estimation of Current and Future Physiological States in Insular Cortex
Livneh, Y., Sugden, A. U., Madara, J. C., Essner, R. A., Flores, V. I., Sugden, L. A., Resch, J. M., Lowell, B. B., & Andermann, M. L. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.027 · Cited by 209
Anterior insular cortex plays a critical role in interoceptive attention
Wang, X., Wu, Q., Egan, L., Gu, X., Liu, P., Gu, H., Yang, Y., Luo, J., Wu, Y., Gao, Z., et al. (2019) · eLife · doi:10.7554/elife.42265 · Cited by 204
Human forebrain activation by visceral stimuli
King, A. B., Menon, R. S., Hachinski, V., & Cechetto, D. F. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991101)413:4 · Cited by 200
García-Cordero, I., Sedeño, L., de la Fuente, L., Slachevsky, A., Forno, G., Klein, F., Lillo, P., Ferrari, J., Rodriguez, C., Bustin, J., et al. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0006 · Cited by 199
Neurobiology of visceral afferent neurons: neuroanatomy, functions, organ regulations and sensations
Jänig, W. (1996) · Biological Psychology · doi:10.1016/0301-0511(95)05145-7 · Cited by 198
Rajendran, P. S., Challis, R. C., Fowlkes, C. C., Hanna, P., Tompkins, J. D., Jordan, M. C., Hiyari, S., Gabris-Weber, B. A., Greenbaum, A., Chan, K. Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09770-1 · Cited by 198
Li, M. M., Madara, J. C., Steger, J. S., Krashes, M. J., Balthasar, N., Campbell, J. N., Resch, J. M., Conley, N. J., Garfield, A. S., & Lowell, B. B. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.028 · Cited by 195
Denton, D. A., Shade, R. E., Zamarripa, F., Egan, G. F., Blair-West, J. R., McKinley, M. J., Lancaster, J. L., & Fox, P. T. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.9.5304 · Cited by 189
Elsenbruch, S., Rosenberger, C., Bingel, U., Forsting, M., Schedlowski, M., & Gizewski, E. R. (2010) · Gastroenterology · doi:10.1053/j.gastro.2010.06.054 · Cited by 187
Interoceptive inference: From computational neuroscience to clinic
Owens, A. P., Allen, M., Ondobaka, S., & Friston, K. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.017 · Cited by 187
Testing the autonomic nervous system
Freeman, R. L., & Chapleau, M. W. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52902-2.00007-2 · Cited by 163
Central Control Circuit for Context-Dependent Micturition
Hou, X. H., Hyun, M., Taranda, J., Huang, K. W., Emmalee, T., Feng, D. D., Atwater, E., Croney, D. M., Zeidel, M. L., Osten, P., et al. (2016) · Cell · doi:10.1016/j.cell.2016.08.073 · Cited by 160
Von Economo neurons in the anterior insula of the macaque monkey.
Evrard, H., Forro, T., & Logothetis, N. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.003 · Cited by 159
Valentino, R. J., Page, M. E., Luppi, P., Zhu, Y., Bockstaele, E. V., & Aston‐Jones, G. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90320-4 · Cited by 148
Self-citationFacets of impulsivity and alcohol use: What role do emotions play?
Herman, A. M., & Duka, T. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.08.011 · Cited by 141
Neurobehavioral evidence of interoceptive sensitivity in early infancy
Maister, L., Tang, T., & Tsakiris, M. (2017) · eLife · doi:10.7554/elife.25318 · Cited by 140
Interoception and Positive Symptoms in Schizophrenia
Ardizzi, M., Ambrosecchia, M., Buratta, L., Ferri, F., Peciccia, M., Donnari, S., Mazzeschi, C., & Gallese, V. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00379 · Cited by 135
Jänig, W., & Häbler, H. (2000) · Progress in brain research · doi:10.1016/s0079-6123(08)62150-0 · Cited by 129
The insular cortex: a comparative perspective
Butti, C., & Hof, P. R. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0264-y · Cited by 125
Anterograde Transneuronal Viral Tracing of Central Viscerosensory Pathways in Rats
Rinaman, L., & Schwartz, G. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5329-03.2004 · Cited by 119
Habenular TCF7L2 links nicotine addiction to diabetes
Duncan, A., Heyer, M. P., Ishikawa, M., Caligiuri, S. P. B., Liu, X.-A., Chen, Z., Micioni Di Bonaventura, M. V., Elayouby, K. S., Ables, J. L., Howe, W. M., et al. (2019) · Nature · doi:10.1038/s41586-019-1653-x · Cited by 119
Ghrelin: From a gut hormone to a potential therapeutic target for alcohol use disorder
Farokhnia, M., Faulkner, M. L., Piacentino, D., Lee, M. R., & Leggio, L. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.02.008 · Cited by 107
Ackerley, R., & Watkins, R. H. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00109.2018 · Cited by 98
CRFergic Innervation Of the Paraventricular Nucleus of the Rat Hypothalamus: A Tract‐Tracing Study
Champagne, D. L., Beaulieu, J., & Drolet, G. (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00179.x · Cited by 94
Neurostimulation methods in the treatment of chronic pain
Moisset, X., Lantéri‐Minet, M., & Fontaine, D. (2019) · Journal of Neural Transmission · doi:10.1007/s00702-019-02092-y · Cited by 91
Pavcovich, L. A., & Valentino, R. J. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)11873-u · Cited by 90
Self-citationIndividual differences in socioemotional sensitivity are an index of salience network function
Toller, G., Brown, J. A., Sollberger, M. A., Shdo, S. M., Bouvet, L., Sukhanov, P., Seeley, W. W., Miller, B. L., & Rankin, K. P. (2018) · Cortex · doi:10.1016/j.cortex.2018.02.012 · Cited by 90
Transneuronal tracing of airways-related sensory circuitry using herpes simplex virus 1, strain H129
McGovern, A. E., Davis-Poynter, N. J., Farrell, M. J., & Mazzone, S. B. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.01.029 · Cited by 89
Feel the Time. Time Perception as a Function of Interoceptive Processing
Lernia, D. D., Serino, S., Pezzulo, G., Pedroli, E., Cipresso, P., & Riva, G. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00074 · Cited by 86
Freeman, S. C., SCOTT, N. W., Powell, R., Johnston, M., Sutton, A. J., & Cooper, N. J. (2018) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2018.02.012 · Cited by 77
Cobos, I., & Seeley, W. W. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht219 · Cited by 71
The mind–body problem: Circuits that link the cerebral cortex to the adrenal medulla
Dum, R. P., Levinthal, D. J., & Strick, P. L. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902297116 · Cited by 71
Recent studies on intestinal vagal afferent innervation. Functional implications
Mei, N. (1983) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(83)90141-8 · Cited by 69
Sensory convergence in the parieto-insular vestibular cortex
Shinder, M. E., & Newlands, S. D. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00731.2013 · Cited by 66
Simmons, A., Strigo, I. A., Matthews, S. C., Paulus, M. P., & Stein, M. B. (2009) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3181a56ed8 · Cited by 64
Autism spectrum disorder and interoception: Abnormalities in global integration?
Hatfield, T. R., Brown, R. F., Giummarra, M. J., & Lenggenhager, B. (2019) · Autism · doi:10.1177/1362361317738392 · Cited by 64
Donofry, S. D., Roecklein, K. A., Wildes, J. E., Miller, M. A., & Erickson, K. I. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.07.011 · Cited by 60
Malik, S., Jacobs, M., Cho, S.-S., Boileau, I., Blumberger, D., Heilig, M., Wilson, A., Daskalakis, Z. J., Strafella, A. P., Zangen, A., et al. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9800-1 · Cited by 58
Stress, Motivation, and the Gut–Brain Axis: A Focus on the Ghrelin System and Alcohol Use Disorder
Morris, L. S., Voon, V., & Leggio, L. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13781 · Cited by 57
Suarez, A. N., Noble, E. E., & Kanoski, S. E. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00101 · Cited by 55
Udit, S., & Gautron, L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00134 · Cited by 53
Contribution of Baroreceptor Function to Pain Perception and Perioperative Outcomes
Suárez-Roca, H., Klinger, R. Y., Podgoreanu, M. V., Ji, R., Sigurdsson, M. I., Waldron, N. H., Mathew, J. P., & Maixner, W. D. (2018) · Anesthesiology · doi:10.1097/aln.0000000000002510 · Cited by 52
Avery, J. A., Powell, J. N., Breslin, F. J., Lepping, R. J., Martin, L. E., Patrician, T. M., Donnelly, J. E., Savage, C. R., & Simmons, W. K. (2017) · Journal of Psychopharmacology · doi:10.1177/0269881117728429 · Cited by 50
Interoceptive awareness in patients with attention-deficit/hyperactivity disorder (ADHD)
Kutscheidt, K., Dresler, T., Hudak, J., Barth, B., Blume, F., Ethofer, T., Fallgatter, A. J., & Ehlis, A. (2019) · ADHD Attention Deficit and Hyperactivity Disorders · doi:10.1007/s12402-019-00299-3 · Cited by 50
Female migraineurs show lack of insular thinning with age
Maleki, N., Barmettler, G., Moulton, E. A., Scrivani, S. J., Veggeberg, R., Spierings, E. L. H., Burstein, R., Becerra, L. R., & Borsook, D. (2015) · Pain · doi:10.1097/j.pain.0000000000000159 · Cited by 49
Stroke and Neurodegeneration Induce Different Connectivity Aberrations in the Insula
Cordero, I. R. G., Sedeño, L., Fraiman, D., Craiem, D. O., de la Fuente, L. A., Salamone, P., Serrano, C. M., Sposato, L. A., Manes, F. F., & Ibáñez, A. M. (2015) · Stroke · doi:10.1161/strokeaha.115.009598 · Cited by 48
Abnormal Sympathetic Reactivity to the Cold Pressor Test in Overweight Humans
Park, J., Middlekauff, H. R., & Campese, V. M. (2012) · American Journal of Hypertension · doi:10.1038/ajh.2012.115 · Cited by 48
Adolescent development of insula‐dependent interoceptive regulation
Li, D., Zucker, N. L., Kragel, P. A., Covington, V. E., & LaBar, K. S. (2016) · Developmental Science · doi:10.1111/desc.12438 · Cited by 47
Migliorini, R., Stewart, J. L., May, A. C., Tapert, S. F., & Paulus, M. P. (2013) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2013.08.015 · Cited by 46
Yang, L., Yang, Y., Yuan, J., Sun, Y., Dai, J., & Su, B. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy286 · Cited by 44
Central nervous system regulation of hepatic lipid and lipoprotein metabolism
Taher, J., Farr, S., & Adeli, K. (2016) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000373 · Cited by 42
Gu, X., Zhou, T., Anagnostou, E. A., Soorya, L. V., Kolevzon, A. L., Hof, P. R., & Fan, J. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13598 · Cited by 42
Significance of neuro-cardiac control mechanisms governed by higher regions of the brain
Taggart, P. I., Critchley, H., van Duijvendoden, S., & Lambiase, P. D. (2016) · Autonomic Neuroscience · doi:10.1016/j.autneu.2016.08.013 · Cited by 38
Altered functional connectivity of interoception in illness anxiety disorder
Grossi, D., Longarzo, M., Quarantelli, M., Salvatore, E., Cavaliere, C., Luca, P. D., Trojano, L., & Aiello, M. (2016) · Cortex · doi:10.1016/j.cortex.2016.10.018 · Cited by 38
Barrera, T., Grubbs, K. M., Kunik, M., & Teng, E. J. (2014) · Journal of clinical psychology in medical settings · doi:10.1007/s10880-014-9393-4 · Cited by 31
The buildup of an urge in obsessive–compulsive disorder: Behavioral and neuroimaging correlates
Stern, E. R., Brown, C., Ludlow, M., Shahab, R., Collins, K., Lieval, A., Tobe, R. H., Iosifescu, D. V., Burdick, K. E., & Fleysher, L. (2020) · Human Brain Mapping · doi:10.1002/hbm.24898 · Cited by 29
Emotional reactivity and interoceptive sensitivity: Exploring the role of age
Mikkelsen, M. B., O’Toole, M. S., Lyby, M. S., Wallot, S., & Mehlsen, M. Y. (2019) · Psychonomic Bulletin & Review · doi:10.3758/s13423-019-01603-y · Cited by 27
Iwai, H., Kuramoto, E., Yamanaka, A., Sonomura, T., Uemura, M., & Goto, T. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.02.045 · Cited by 22
Modulation of Body Representation Impacts on Efferent Autonomic Activity
D’Alonzo, M., Mioli, A., Formica, D., & Pino, G. D. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01532 · Cited by 20
Optogenetic manipulation of ENS - The brain in the gut
Wang, W. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.11.010 · Cited by 13
Barone, F. C., de Coronado, I. Z., & Wayner, M. J. (1995) · Brain Research Bulletin · doi:10.1016/0361-9230(95)00096-w · Cited by 12
Zaman, J., van de Pavert, I., Oudenhove, L. V., & Diest, I. V. (2019) · Psychophysiology · doi:10.1111/psyp.13494 · Cited by 11
The concept of homeostasis in medicine.
Wiener, N. (1953) · PubMed · Cited by 6
Cited by
Sorted by citations
Neural circuits of interoception
Berntson, G. G., & Khalsa, S. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.011 · Cited by 419
Cardiogenic control of affective behavioural state
Hsueh, B., Chen, R., Jo, Y., Tang, D., Raffiee, M., Kim, Y. S., Inoue, M., Randles, S., Ramakrishnan, C., Patel, S., et al. (2023) · Nature · doi:10.1038/s41586-023-05748-8 · Cited by 335
The role of the salience network in cognitive and affective deficits
Schimmelpfennig, J., Topczewski, J., Zajkowski, W. K., & Jankowiak-Siuda, K. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1133367 · Cited by 379
Anterior insula as a gatekeeper of executive control
Molnar-Szakacs, I., & Uddin, L. Q. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104736 · Cited by 333
Interventions and Manipulations of Interoception
Weng, H. Y., Feldman, J. L., Leggio, L., Napadow, V., Park, J., & Price, C. J. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.010 · Cited by 250
Metadata
- Authors
- Chen, W. G., Schloesser, D., Arensdorf, A. M., Simmons, J. M., Cui, C., Valentino, R., Gnadt, J. W., Nielsen, L., Hillaire-Clarke, C. S., Spruance, V., Horowitz, T. S., Vallejo, Y. F., & Langevin, H. M.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Chen, Wen G.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2021-01
- Volume
- 44
- Issue
- 1
- Pages
- 3-16
- ISSN
- 0166-2236 (ISSN-L)
- PMC
- PMC7780231
- OpenAlex
- W3115649676
- Cited by
- 707
- References
- 119
- Citations by year
- 2026: 145 · 2025: 155 · 2024: 138 · 2023: 133 · 2022: 85 · 2021: 48
- FWCI
- 11.16
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Trends in Neurosciences (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH Blueprint for Neuroscience Research
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Rate Variability and Autonomic Control
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Keywords
- interoception, interoceptive signals, signal integration, neural pathways, predictive modeling, research framework
- MeSH terms
- Humans, Interoception
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review